Studies on the actin-binding protein HS1 in platelets

Thomas, S.G., Calaminus, S.D., Auger, J.M., Watson, S.P. and Machesky, L. M. (2007) Studies on the actin-binding protein HS1 in platelets. BMC Cell Biology, 8, 46. (doi: 10.1186/1471-2121-8-46) (PMID:17996076) (PMCID:PMC2203996)

Abstract

Background The platelet cytoskeleton mediates the dramatic change in platelet morphology that takes place upon activation and stabilizes thrombus formation. The Arp2/3 complex plays a vital role in these processes, providing the protrusive force for lamellipodia formation. The Arp2/3 complex is highly regulated by a number of actin-binding proteins including the haematopoietic-specific protein HS1 and its homologue cortactin. The present study investigates the role of HS1 in platelets using HS1-/- mice. Results The present results demonstrate that HS1 is not required for platelet activation, shape change or aggregation. Platelets from HS1-/- mice spread normally on a variety of adhesion proteins and have normal F-actin and Arp2/3 complex distributions. Clot retraction, an actin-dependent process, is also normal in these mice. Platelet aggregation and secretion is indistinguishable between knock out and littermates and there is no increase in bleeding using the tail bleeding assay. Conclusion This study concludes that HS1 does not play a major role in platelet function. It is possible that a role for HS1 is masked by the presence of cortactin.

• Item Type: Articles
• Status: Published
• Refereed: Yes
• Glasgow Author(s) Enlighten ID: Machesky, Professor Laura
• Authors: Thomas, S.G., Calaminus, S.D., Auger, J.M., Watson, S.P., and Machesky, L. M.
• College/School: College of Medical Veterinary and Life Sciences > School of Cancer Sciences
• Journal Name: BMC Cell Biology
• Publisher: Biomed Central
• ISSN: 1471-2121
• Copyright Holders: Copyright © 2007 Thomas et al.
• First Published: First published in BMC Cell Biology 8:46
• Publisher Policy: Reproduced under a Creative Commons licence